EP2 Polyclonal Antibody, 100ul[BT-AP02979] Nucleic Acid Amplification Defects in TMEM237 are a

Defects in TMEM237 are a cause of Joubert syndrome-14

Retention of resident soluble proteins in the lumen of the endoplasmic reticulum (ER) is achieved in both yeast and animal cells by their continual retrieval from the cis-Golgi

they are transmembrane proteins containing 2 immunoglobulin (Ig)-like domains and 2 type I thrombospondin motifs in the extracellular region

The protein encoded by PRKAG1 (protein kinase AMP-activated non-catalytic subunit gamma 1) is a regulatory subunit of the AMP-activated protein kinase (AMPK)

EP2 Polyclonal Antibody, 100ul[BT-AP02979] Nucleic Acid Amplification Defects in TMEM237 are aPTGER2 (prostaglandin E receptor 2) encodes a receptor for prostaglandin E2, a metabolite of arachidonic acid which has different biologic activities in a wide range of tissues. Mutations in PTGER2 are associated with aspirin induced susceptibility to asthma.